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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601082Generated: October 25, 2026

Ammonium Chloride → Benzenemethanol, alpha-1-propen-1-yl-

https://huagongshe.com/reaction/601082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantCrotonaldehydeHCID 447466—
ReactantHCID 178418255HCID 178418255—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductBenzenemethanol, alpha-1-propen-1-yl-HCID 21967499.9%

Reaction Steps

To a cooled (0-55° C.) 927 mL of 1 M solution of phenyl magnesium bromide in tetrahydofuran was added dropwise a solution of crotonaldehyde (65.0 g) in 130 mL of anhydrous ether over a period of 2 hours and 45 minutes. The reaction was stirred for an additional 45 minutes and then warmed to room temperature. After four more hours of stirring, saturated ammonium chloride aqueous solution (750 mL) was added to the reaction. The mixture was extracted with 750 mL of ether twice. The combined extract was dried over anhydrous potassium carbonate and filtered. The solvent was evaporated to give 135.88 g (99.9%) of the desired 1-phenyl-2-buten-1-ol as an oil which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902259B2
Source datasetuspto-grants-2011_03
ORD IDord-b3d8af6edac34ac28fd730ced29100ef
Source noteuspto-grants-2011_03